Allele Registry

Canonical Allele Identifier: PA2829583135

Gene: SLC12A6 HGNC NCBI

ClinVar RCV:

RCV001957250

RCV002560471

ClinVar Variation:

1424771

HGVS (amino-acid)	Matching Registered Transcripts
NP_005126.1:p.Trp159Cys	CA391612685 NM_005135.2:c.477G>T CA391612688 NM_005135.2:c.477G>C